A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892961



Internal ID19183781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:13635911..13768583hg38UCSC Ensembl
Outerchr17:13635911..13768583hg38UCSC Ensembl
Innerchr17:13539228..13671900hg19UCSC Ensembl
Outerchr17:13539228..13671900hg19UCSC Ensembl
Innerchr17:13479953..13612625hg18UCSC Ensembl
Outerchr17:13479953..13612625hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38132673
hg19132673
hg18132673
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782083
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892961
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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